I have recently been diagnosed with OA and with palindromic arthritis (possibly developing into RA?) by Rheumatologist, who has asked me to consider starting Sulfasalazine. My blood tests are negative. I am interested in comparing my symptoms with what people experienced right at the onset of their RA. Although I had inflammation in fingers and knees when it all started in January, presently I have some pain developing in joints not previously affected (elbow and shoulder) but no inflammation there.
Thanks for any comments.
Written by
mchemery
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Im sorry did not see your post the other day sadly it happens! I had to look up the arthritis you were diagnosed with and found this info on the subject.
Hi Batty1. Thank you so much for the link which explains clearly and concisely what Palindromic Arthritis is. It mentions that 50% of people diagnosed with this are likely to develop RA, something I didn't know. I was going to wait a little longer to start the Sulfasalzine which my Rheumatologist prescribed (I haven't taken any medication in my whole life) but I think I should consider starting soon. Once again thank you :-))
I have psoriatic arthritis and if I didn’t inject monthly I would still be bedridden and house bound and my PSA came out of the blue after thyroidectomy 4 years ago which ruined my health.
I get the medication is scary and like all medications it probably won’t be a smooth ride and maybe really researching Sulfasalazine is needed before you commit.
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